Evidence map›Paper›PMID 39996476›Full record

ArticleHuman vaccines & immunotherapeutics2025

Immunotherapy-induced microsatellite instability status shift in recurrent perihilar cholangiocarcinoma: A case report.

Hailing Yu, Tan Deng, Hongbing Liu

Abstract readCase Reports
In one paragraph

Article in Human vaccines & immunotherapeutics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Hailing YuDepartment of Oncology, Hunan Provincial People's Hospital (The First Affiliated Hospital of Hunan Normal University), Changsha, Hunan, China.
Tan DengDepartment of Oncology, Hunan Provincial People's Hospital (The First Affiliated Hospital of Hunan Normal University), Changsha, Hunan, China.
Hongbing LiuDepartment of Oncology, Xiangtan First People's Hospital, Changsha, Hunan, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immunotherapy revolutionized the treatment of biliary tract tumors and tumors with high microsatellite instability (MSI-H). This paper reports a 52-year-old woman with recurrent perihilar cholangiocarcinoma. The tumor was initially microsatellite stable (MSS) and proficient mismatch repair (pMMR) but shifted to MSI-H and deficient mismatch repair (dMMR) after combined immunotherapy. Following laparoscopic radical resection for jaundice, stage IV recurrence was diagnosed. Genetic testing revealed the MSS status. Subsequent treatment with camrelizumab and lenvatinib led to a partial response. Ovarian metastases, removed due to abdominal symptoms, exhibited dMMR and MSI-H. The mismatch in MSI status between the primary tumor and metastases suggests tumor heterogeneity and the influence of spatial or temporal factors. This shift can have important clinical significance since MSI-H is associated with significant responses to immune checkpoint inhibitors. MSI-H should be systematically tested in tumors and metastases to personalize treatments. MSI heterogeneity is not only rare but potentially has implications for treatment personalization and prognosis in patients with cholangiocarcinoma. This case highlights the dynamic changes in tumor characteristics during immunotherapy.

Indexed as

Bile Duct NeoplasmsCholangiocarcinomaImmunotherapyKlatskin TumorMicrosatellite InstabilityNeoplasm Recurrence, LocalAntibodies, Monoclonal, HumanizedDNA Mismatch RepairFemaleHumansImmune Checkpoint InhibitorsMiddle AgedAntibodies, Monoclonal, HumanizedcamrelizumabImmune Checkpoint Inhibitorscase reportcombined immunotherapymicrosatellite instability statusRecurrent perihilar cholangiocarcinomatumor heterogeneity

Identifiers

PMID39996476
PMCPMC11864312

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.